The Basics of Myasthenia Gravis (2024)

What Is Myasthenia Gravis?

Myasthenia gravis is a chronic condition that causes muscles to tire and weaken easily. For example, if you have myasthenia gravis, you may notice that during a meal, your jaw muscles become tired and weak, interfering with your ability to chew food. After you have rested for a little while, the muscles may become strong again, allowing you to resume eating.

This waxing-and-waning weakness of muscles, worsening with use and improving with rest, is a hallmark of this disease. There typically are periods when you may notice more symptoms (called an exacerbation), interspersed with periods when symptoms decrease or disappear (remission).

Myasthenia gravis affecting multiple muscle groups throughout the body is called generalized myasthenia gravis. Other common muscle groups that are affected may make it difficult for you to chew, swallow, smile, shrug, lift your arm up, grip, rise to a stand, or walk up stairs. When the muscles needed for breathing are affected, a patient is said to be in myasthenic crisis. This is a life-threatening situation.

Though anyone can get myasthenia gravis, those most likely to do so are women between ages 20 and 40 or men between ages 50 and 70. If a woman with myasthenia gravis gives birth, the baby may have some temporary, and potentially life-threatening, muscle weakness (neonatal myasthenia) because of antibodies that have transferred from the mother's bloodstream. Typically, during the baby's first weeks of life, the antibodies are cleared from the baby's circulation and the baby develops normal muscle tone and strength.

Myasthenia Gravis Symptoms

The disease most commonly affects muscles that control eye and eyelid movement, so the first symptoms you notice may be eyelid drooping and/or blurred or doubled vision. The majority will go on to have weakness in other muscle groups in 1 or 2 years.

General symptoms of myasthenia gravis include:

  • Weakness in your eye muscles
  • Drooping eyelids
  • Double vision
  • Blurred vision
  • Change in your facial expression
  • Trouble swallowing
  • Shortness of breath
  • Problems speaking
  • Problems walking and lifting things
  • Trouble holding up your head

If the muscles you use to breathe get weak enough that you can’t control them, it’s called a myasthenic crisis. This is a medical emergency that may requirea ventilator to help you breathe. Around 15% to 20% of people with myasthenia gravis have at least one myasthenic crisis. They can be caused by an infection, stress, surgery, or a reaction to medication.

Myasthenia Gravis Causes

Under normal conditions, nerves direct your muscles to work by sending a message through an area called a receptor. The chemical that delivers the message is called acetylcholine. When acetylcholine binds to a nerve receptor, your muscle knows to contract. In myasthenia gravis, your body attacks its acetylcholine receptors.

Myasthenia gravis is considered to be an autoimmune disorder. In an autoimmune disease, some of the body's antibodies (special proteins in your body that are supposed to be programmed to fight foreign invaders such as bacteria, viruses, or fungi) mistake a part of your own body as foreign, resulting in its destruction. In the case of myasthenia gravis, antibodies block, attack or destroy the acetylcholine receptors needed for muscle contraction.

No one knows exactly what causes the body to begin producing the antibodies that destroy acetylcholine receptors. In some cases, the process seems to be related to the thymus gland, which helps produce antibodies.

About 15% of all myasthenia gravis patients are found to have a thymoma, a tumor of the thymus. Although most thymomas are benign (not cancerous), the thymus is usually removed (thymectomy) to prevent the potential spread of cancer. In fact, thymectomy seems to improve symptoms of myasthenia gravis in some patients, even if no tumor is present.

Myasthenia Gravis Diagnosis

To see if you have myasthenia gravis, your doctor will start with a neurological exam. This includes a test of your:

  • Reflexes
  • Muscle strength
  • Muscle tone
  • Touch
  • Sight
  • Coordination
  • Balance
  • Fatigability (how soon your muscles weaken)

Then you’ll have tests to help look more closely at symptoms of myasthenia gravis. These include:

  • Edrophonium test. Your doctor injects you with a chemical called edrophonium chloride to see if it improves your muscle strength. If it does, that’s a sign you might have myasthenia gravis.
  • Ice pack test. If you have a drooping eyelid, your doctor may put an ice pack on it for 2 minutes to see if the low temperature has an effect on it.
  • Blood test. Your doctor will draw some of your blood and send it to a lab to check for certain antibodies that affect muscle nerve receptors.
  • Repetitive nerve stimulation. This test uses electrodes on your muscles to send small electrical pulses to see if your nerves react to the signals.
  • Single-fiber electromyography (EMG). Your doctor puts a thin wire electrode through your skin and into a muscle. It can test the electrical activity between your brain and your muscles.
  • Imaging. Your doctor may suggest a CT scan or MRI to look more closely for a tumor on your thymus that could be causing symptoms.
  • Pulmonary functioning tests. Your doctor tests your breathing to see if your lungs are affected by myasthenia gravis.

Myasthenia Gravis Treatment and Home Remedies

Your treatment will depend on your age, how severe your symptoms are, and how fast the condition is progressing. You might need one or several treatments together. Your doctor may recommend a medication such as:

  • Cholinesterase inhibitors. These medications boost the communication between your nerves and your muscles. They can help strengthen muscles.
  • Corticosteroids. Corticosteroids such as prednisone mute your immune system and slow the release of antibodies that could be helping block your nerve receptors.
  • Immunosuppressants. Your doctor may add immunosuppressants to your corticosteroids to help reduce your immune system response.
  • Neonatal Fc receptor blocker.It works by blocking theautoantibodies that cause myasthenia gravis and helps ease the symptoms.

If you’re dealing with a sudden worsening of symptoms or will soon have surgery or other therapies, your doctor may recommend intravenous (IV) therapy. Choices for this include:

  • Plasmapheresis. This procedure is like dialysis, because it filters your blood. Your blood goes through a machine that removes certain antibodies. The effects are faster than other treatments but theyare not long lasting (about a month). This procedure is usually used in a crisis.
  • Intravenous immunoglobulin (IVIg). This therapy injects new antibodies into your bloodstream. These antibodies alter your immune system response to help with symptoms. Results typically last about 3-6 weeks.
  • Monoclonal antibodies. Your doctor will likely recommend this option only if other treatments haven’t worked. They can have serious side effects.

If your myasthenia gravis is due to a tumor on your thymus gland, you may need surgery to remove the whole gland (thymectomy). Even if you don’t have a tumor, taking your thymus out may help ease your symptoms. It may take years to see benefits from a thymectomy.

You may need open surgery to remove your thymus. A surgeon opens your breastbone to get to your thymus and take it out.

Another option that may work is minimally invasive surgery. There are two options:

  • Video-assisted thymectomy. Surgeons make small cuts in your neck or chest and use a long, thin camera called an endoscope along with instruments to take out your thymus.
  • Robot-assisted thymectomy. Surgeons make the same small cuts as video-assisted thymectomy and then use a robot with a camera and mechanical arms to remove your thymus.

In addition to medical treatments, you can make lifestyle changes to help manage your myasthenia gravis symptoms, including:

  • Save energy when you eat. If chewing is a struggle, eat at times when you have the most strength. You might find it easier to eat several small meals a day instead of longer, larger ones less often. Stick to soft foods, and take breaks between bites.
  • Install safety aids. Put handrails anywhere you might need a helpful handle, like next to the toilet or near tables. Remove any tripping risks such as rugs or floor clutter.
  • Let machines do the work. Switch to an electric toothbrush and can opener, or any other device that can save you strength.
  • Wear an eye patch. It can help with double vision. Use one when you watch TV or read, and switch eyes from time to time.
  • Plan ahead. Be smart with your strength. Do chores or errands when you feel best during the day.
The Basics of Myasthenia Gravis (2024)

FAQs

What is the basis of myasthenia gravis? ›

MG is caused by antibodies against the acetylcholine receptor (AChR), which produce a compromise in the end-plate potential, reducing the safety factor for effective synaptic transmission. It is clear that AChR antibody destruction of the postsynaptic surface is dependent on complement activation.

What are 3 factors that can make myasthenia gravis worse? ›

Factors that can make myasthenia gravis worse include:
  • Fatigue.
  • Illness or infection.
  • Surgery.
  • Stress.
  • Some medicines — such as beta blockers, quinidine gluconate, quinidine sulfate, quinine (Qualaquin), phenytoin (Dilantin), certain anesthetics and some antibiotics.
  • Pregnancy.
  • Menstrual periods.
Jun 22, 2023

Can you lead a normal life with MG? ›

Thanks to advances in diagnosis and treatment, many people with myasthenia gravis , a rare autoimmune neuromuscular disorder, can expect to lead a normal or near-normal life.

What famous person has myasthenia gravis? ›

Famous People
  • David Niven.
  • Aristotle Onassis.
  • Sir Lawrence Olivier.
  • Phil Silvers (actor – Sgt. Bilko)

What is myasthenia gravis in layman's terms? ›

People with myasthenia gravis (MG) have muscle weakness that worsens throughout the day. This autoimmune disease affects the neuromuscular system. Drooping eyelids are often the first sign. Eventually, you may find it difficult to control your neck and limbs.

How the doctors know the difference between myasthenia gravis and ALS? ›

Diagnostic tests such as an MRI, nerve studies, and blood tests will be a part of determining if someone has either MG or ALS, and these tests are vital so that the proper treatment can begin. Since ALS and MG have drastically different outcomes, a person must begin therapy as soon as possible.

What is the greatest danger of myasthenia gravis? ›

Myasthenia gravis causes a significant number of complications. These include myasthenic crisis, an acute respiratory paralysis that requires intensive care, as well as adverse events due to long term medication treatment like opportunistic infections and lymphoproliferative malignancies.

What is the main cause of death in myasthenia gravis? ›

As MG progresses, it can affect the muscles involved in breathing. When these muscles are affected, it can become harder to breathe. This can become so severe that a person cannot breathe on their own. This is considered a crisis and can lead to death.

Can you drink coffee with myasthenia gravis? ›

Some people find that drinking alcohol makes their symptoms worse. Other people find that drinks with caffeine, such as coffee, tea, and sodas, aggravate their diarrhea. Many find meat hard to chew or that certain foods make them choke.

Who is the best doctor for myasthenia gravis? ›

Rheumatologist. A rheumatologist specializes in treating autoimmune conditions like myasthenia gravis. This doctor may work with a neurologist to help find the right combination of treatments for a person with MG. Having a rheumatologist is especially important for people that have more than 1 autoimmune disorder.

What should I avoid with MG? ›

Drugs to avoid or use with caution in MG*
  • Telithromycin: antibiotic for community acquired pneumonia. ...
  • Fluoroquinolones (e.g., ciprofloxacin, moxifloxacin and levofloxacin): commonly prescribed broadspectrum antibiotics that are associated with worsening MG. ...
  • Botulinum toxin: avoid.

What are interesting facts about myasthenia gravis? ›

What is myasthenia gravis?
  • Myasthenia is an autoimmune disease. ...
  • Myasthenia gravis happens most often in women ages 20 to 40 and men ages 50 to 80, but it can happen at any age.
  • Your muscles become unusually tired and weak after exercise.
  • You have drooping eyelids and double vision.

What disease is similar to myasthenia gravis? ›

Those that mimic MG include oculopharyngeal dystrophy and myotonic dystrophy. Muscle disorders characterized by muscle inflammation that mimic MG include dermatomyositis and polymyositis.

Is myasthenia gravis high risk COVID? ›

In the CARE-MG (COVID-19 Associated Risks and Effects in Myasthenia Gravis) registry, a physician-reported registry on outcomes of patients with MG and COVID-19, preliminary data from 91 patients showed a high risk of hospitalization (69%), MG exacerbation (40%), and death (24%).

What factors cause myasthenia? ›

Curare, aminoglycosides, quinine, procainamide, and calcium channel blockers are other drugs that might cause myasthenia-like weakness or aggravate weakness in patients with MG. Fatigue, illness, infection, surgery, stress, pregnancy, and menstruation are other factors that might exacerbate MG.

What is the basis of treatment for myasthenia gravis? ›

There is no cure for myasthenia gravis, but it is treated with medications and sometimes surgery. You may be put on a drug called pyridostigmine (Mestinon), that increases the amount of acetylcholine available to stimulate the receptors.

What is the difference between myasthenia gravis and multiple sclerosis? ›

Myasthenia gravis and multiple sclerosis are autoimmune diseases that affect the neuromuscular junctions and central nervous system (CNS), respectively. The main mechanism of myasthenia gravis is antibody-mediated, while that of multiple sclerosis is T cell-mediated.

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